Allele Registry

Canonical Allele Identifier: PA891866338

Gene: FBXW7 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000419147

RCV000420198

RCV000421262

RCV000421492

RCV000426581

RCV000428024

RCV000429882

RCV000431326

RCV000436581

RCV000437252

RCV000437918

RCV000439102

RCV000441574

RCV000443495

ClinVar Variation:

376418

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336727.1:p.Arg465Gly	CA16602855 NM_001349798.2:c.1393C>G